A citation-based method for searching scientific literature

Joan Scott, Tracy Trotter. Pediatrics 2013
Times Cited: 15







List of co-cited articles
43 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



Genetic services and attitudes in primary care pediatrics.
Michael L Rinke, Natalie Mikat-Stevens, Robert Saul, Amy Driscoll, Jill Healy, Beth A Tarini. Am J Med Genet A 2014
23
33

A systematic review of interventions to provide genetics education for primary care.
Milena Paneque, Daniela Turchetti, Leigh Jackson, Peter Lunt, Elisa Houwink, Heather Skirton. BMC Fam Pract 2016
39
26




Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectives.
Elisa Jf Houwink, Scheltus J van Luijk, Lidewij Henneman, Cees van der Vleuten, Geert Jan Dinant, Martina C Cornel. BMC Fam Pract 2011
80
20

A Quality Improvement Collaborative to Improve Pediatric Primary Care Genetic Services.
Michael L Rinke, Amy Driscoll, Natalie Mikat-Stevens, Jill Healy, Elizabeth Colantuoni, Abdallah F Elias, Beth A Pletcher, Ruth S Gubernick, Ingrid Larson, Wendy K Chung,[...]. Pediatrics 2016
7
42

Primary Care Providers' Initial Evaluation of Children with Global Developmental Delay: A Clinical Vignette Study.
Beth A Tarini, Brian J Zikmund-Fisher, Howard M Saal, Laurie Edmondson, Wendy R Uhlmann. J Pediatr 2015
10
30


Survey of family history taking and genetic testing in pediatric practice.
Robert A Saul, Tracy Trotter, Kerry Sease, Beth Tarini. J Community Genet 2017
12
25

Why rare diseases are an important medical and social issue.
Arrigo Schieppati, Jan-Inge Henter, Erica Daina, Anita Aperia. Lancet 2008
251
13

Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes.
Sibel Kantarci, Lihadh Al-Gazali, R Sean Hill, Dian Donnai, Graeme C M Black, Eric Bieth, Nicolas Chassaing, Didier Lacombe, Koen Devriendt, Ahmad Teebi,[...]. Nat Genet 2007
199
13

Evolving importance of kidney disease: from subspecialty to global health burden.
Kai-Uwe Eckardt, Josef Coresh, Olivier Devuyst, Richard J Johnson, Anna Köttgen, Andrew S Levey, Adeera Levin. Lancet 2013
570
13

INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy.
Olivia Boyer, Fabien Nevo, Emmanuelle Plaisier, Benoit Funalot, Olivier Gribouval, Geneviève Benoit, Evelyne Huynh Cong, Christelle Arrondel, Marie-Josèphe Tête, Rodrick Montjean,[...]. N Engl J Med 2011
161
13

Genotype-phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease.
Erick Denamur, Anne-Lise Delezoide, Corinne Alberti, Agnès Bourillon, Marie-Claire Gubler, Raymonde Bouvier, Olivier Pascaud, Jacques Elion, Bernard Grandchamp, Laurence Michel-Calemard,[...]. Kidney Int 2010
52
13

Challenges of translating genetic tests into clinical and public health practice.
Wolf H Rogowski, Scott D Grosse, Muin J Khoury. Nat Rev Genet 2009
77
13


Renal involvement in mitochondrial cytopathies.
Francesco Emma, Enrico Bertini, Leonardo Salviati, Giovanni Montini. Pediatr Nephrol 2012
66
13

Characterization of PKD protein-positive exosome-like vesicles.
Marie C Hogan, Luca Manganelli, John R Woollard, Anatoliy I Masyuk, Tatyana V Masyuk, Rachaneekorn Tammachote, Bing Q Huang, Alexey A Leontovich, Thomas G Beito, Benjamin J Madden,[...]. J Am Soc Nephrol 2009
211
13

Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics.
Bruce R Korf, Anna B Berry, Melvin Limson, Ali J Marian, Michael F Murray, P Pearl O'Rourke, Eugene R Passamani, Mary V Relling, John Tooker, Gregory J Tsongalis,[...]. Genet Med 2014
79
13


Family history in pediatric primary care.
Tracy L Trotter, Helen M Martin. Pediatrics 2007
30
13

Protocol for implementation of family health history collection and decision support into primary care using a computerized family health history system.
Lori A Orlando, Elizabeth R Hauser, Carol Christianson, Karen P Powell, Adam H Buchanan, Blair Chesnut, Astrid B Agbaje, Vincent C Henrich, Geoffrey Ginsburg. BMC Health Serv Res 2011
33
13

The family history--more important than ever.
Alan E Guttmacher, Francis S Collins, Richard H Carmona. N Engl J Med 2004
344
13

Family history in primary care pediatrics.
Beth A Tarini, Joseph D McInerney. Pediatrics 2013
14
14

CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
Brian H Shirts, Joseph S Salama, Samuel J Aronson, Wendy K Chung, Stacy W Gray, Lucia A Hindorff, Gail P Jarvik, Sharon E Plon, Elena M Stoffel, Peter Z Tarczy-Hornoch,[...]. J Am Med Inform Assoc 2015
56
13

How to know when physicians are ready for genomic medicine.
Jason L Vassy, Bruce R Korf, Robert C Green. Sci Transl Med 2015
41
13

Developing knowledge resources to support precision medicine: principles from the Clinical Pharmacogenetics Implementation Consortium (CPIC).
James M Hoffman, Henry M Dunnenberger, J Kevin Hicks, Kelly E Caudle, Michelle Whirl Carrillo, Robert R Freimuth, Marc S Williams, Teri E Klein, Josh F Peterson. J Am Med Inform Assoc 2016
50
13

The medical home.
. Pediatrics 2002
599
13

Practical considerations in genomic decision support: The eMERGE experience.
Timothy M Herr, Suzette J Bielinski, Erwin Bottinger, Ariel Brautbar, Murray Brilliant, Christopher G Chute, Beth L Cobb, Joshua C Denny, Hakon Hakonarson, Andrea L Hartzler,[...]. J Pathol Inform 2015
31
13

Adoption of pharmacogenomic testing by US physicians: results of a nationwide survey.
E J Stanek, C L Sanders, K A Johansen Taber, M Khalid, A Patel, R R Verbrugge, B C Agatep, R E Aubert, R S Epstein, F W Frueh. Clin Pharmacol Ther 2012
266
13

Attitudes of clinicians following large-scale pharmacogenomics implementation.
J F Peterson, J R Field, Y Shi, J S Schildcrout, J C Denny, T L McGregor, S L Van Driest, J M Pulley, I M Lubin, M Laposata,[...]. Pharmacogenomics J 2016
47
13

Genomic medicine: a decade of successes, challenges, and opportunities.
Jeanette J McCarthy, Howard L McLeod, Geoffrey S Ginsburg. Sci Transl Med 2013
137
13

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
534
13

Determining the effects and challenges of incorporating genetic testing into primary care management of hypertensive patients with African ancestry.
C R Horowitz, N S Abul-Husn, S Ellis, M A Ramos, R Negron, M Suprun, R E Zinberg, T Sabin, D Hauser, N Calman,[...]. Contemp Clin Trials 2016
25
13

Integration of Genomics in Primary Care.
Eric A Larson, Russell A Wilke. Am J Med 2015
18
13

'Someday it will be the norm': physician perspectives on the utility of genome sequencing for patient care in the MedSeq Project.
Jason L Vassy, Kurt D Christensen, Melody J Slashinski, Denise M Lautenbach, Sridharan Raghavan, Jill Oliver Robinson, Jennifer Blumenthal-Barby, Lindsay Zausmer Feuerman, Lisa Soleymani Lehmann, Michael F Murray,[...]. Per Med 2015
27
13

Providers' knowledge of genetics: A survey of 5915 individuals and families with genetic conditions.
Erin K Harvey, Chana E Fogel, Mark Peyrot, Kurt D Christensen, Sharon F Terry, Joseph D McInerney. Genet Med 2007
56
13

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
13

Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic Experience.
Konstantinos N Lazaridis, Kimberly A Schahl, Margot A Cousin, Dusica Babovic-Vuksanovic, Douglas L Riegert-Johnson, Ralitza H Gavrilova, Tammy M McAllister, Noralane M Lindor, Roshini S Abraham, Michael J Ackerman,[...]. Mayo Clin Proc 2016
61
13

Views Of Primary Care Providers On Testing Patients For Genetic Risks For Common Chronic Diseases.
Diane Hauser, Aniwaa Owusu Obeng, Kezhen Fei, Michelle A Ramos, Carol R Horowitz. Health Aff (Millwood) 2018
26
13

Making Personalized Health Care Even More Personalized: Insights From Activities of the IOM Genomics Roundtable.
Sean P David, Samuel G Johnson, Adam C Berger, W Gregory Feero, Sharon F Terry, Larry A Green, Robert L Phillips, Geoffrey S Ginsburg. Ann Fam Med 2015
20
13

Urinary proteome analysis to exclude severe vesicoureteral reflux.
Jens Drube, Eric Schiffer, Esther Lau, Claus Petersen, Martin Kirschstein, Markus J Kemper, Ralf Lichtinghagen, Benno Ure, Harald Mischak, Lars Pape,[...]. Pediatrics 2012
21
6

STEC-HUS, atypical HUS and TTP are all diseases of complement activation.
Marina Noris, Federica Mescia, Giuseppe Remuzzi. Nat Rev Nephrol 2012
240
6

Single-cell sequencing-based technologies will revolutionize whole-organism science.
Ehud Shapiro, Tamir Biezuner, Sten Linnarsson. Nat Rev Genet 2013
580
6

Atypical hemolytic-uremic syndrome.
Marina Noris, Giuseppe Remuzzi. N Engl J Med 2009
787
6

A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis.
M Town, G Jean, S Cherqui, M Attard, L Forestier, S A Whitmore, D F Callen, O Gribouval, M Broyer, G P Bates,[...]. Nat Genet 1998
381
6

Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndrome.
Kálmán Tory, Dóra K Menyhárd, Stéphanie Woerner, Fabien Nevo, Olivier Gribouval, Andrea Kerti, Pál Stráner, Christelle Arrondel, Evelyne Huynh Cong, Tivadar Tulassay,[...]. Nat Genet 2014
85
6

Inducible podocyte injury and proteinuria in transgenic zebrafish.
Weibin Zhou, Friedhelm Hildebrandt. J Am Soc Nephrol 2012
83
6


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.